JP5973739B2 - 積層セラミック部品製造用溶剤又は溶剤組成物 - Google Patents
積層セラミック部品製造用溶剤又は溶剤組成物 Download PDFInfo
- Publication number
- JP5973739B2 JP5973739B2 JP2012018186A JP2012018186A JP5973739B2 JP 5973739 B2 JP5973739 B2 JP 5973739B2 JP 2012018186 A JP2012018186 A JP 2012018186A JP 2012018186 A JP2012018186 A JP 2012018186A JP 5973739 B2 JP5973739 B2 JP 5973739B2
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- JP
- Japan
- Prior art keywords
- ether
- glycol
- butyl
- methylbutyl
- dimethylpropyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000002904 solvent Substances 0.000 title claims description 66
- 239000000919 ceramic Substances 0.000 title claims description 42
- 239000000203 mixture Substances 0.000 title claims description 31
- 238000004519 manufacturing process Methods 0.000 claims description 16
- 239000003985 ceramic capacitor Substances 0.000 claims description 3
- VRVNDPOBMUHUBY-UHFFFAOYSA-N 1-[2-(2-methoxypropoxy)propoxy]-2-methylpropane Chemical compound C(C(C)C)OCC(OCC(C)OC)C VRVNDPOBMUHUBY-UHFFFAOYSA-N 0.000 claims description 2
- HBUKXWXYJOMLIP-UHFFFAOYSA-N 1-[2-(2-methoxypropoxy)propoxy]-3-methylbutane Chemical compound C(CC(C)C)OCC(OCC(C)OC)C HBUKXWXYJOMLIP-UHFFFAOYSA-N 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 91
- -1 terpineol hydrogenated acetate Chemical class 0.000 description 90
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 73
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 70
- 125000000217 alkyl group Chemical group 0.000 description 64
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 49
- 229920005989 resin Polymers 0.000 description 40
- 239000011347 resin Substances 0.000 description 40
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 38
- 239000011230 binding agent Substances 0.000 description 32
- 239000011248 coating agent Substances 0.000 description 25
- 238000000576 coating method Methods 0.000 description 25
- 235000013772 propylene glycol Nutrition 0.000 description 25
- 238000000034 method Methods 0.000 description 20
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 19
- 239000001856 Ethyl cellulose Substances 0.000 description 18
- 229920001249 ethyl cellulose Polymers 0.000 description 18
- 235000019325 ethyl cellulose Nutrition 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 13
- 239000003960 organic solvent Substances 0.000 description 12
- 239000004020 conductor Substances 0.000 description 11
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 9
- 238000001035 drying Methods 0.000 description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 9
- 238000009835 boiling Methods 0.000 description 8
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 8
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 239000011354 acetal resin Substances 0.000 description 6
- 150000005215 alkyl ethers Chemical class 0.000 description 6
- 239000003990 capacitor Substances 0.000 description 6
- 238000010304 firing Methods 0.000 description 6
- 229920006324 polyoxymethylene Polymers 0.000 description 6
- 229920002554 vinyl polymer Polymers 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- AQZGPSLYZOOYQP-UHFFFAOYSA-N Diisoamyl ether Chemical compound CC(C)CCOCCC(C)C AQZGPSLYZOOYQP-UHFFFAOYSA-N 0.000 description 4
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
- 229940116411 terpineol Drugs 0.000 description 4
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 4
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 description 3
- ZSUGETUFOUXQCL-UHFFFAOYSA-N 2-(3-methylhexan-3-yloxy)ethanol Chemical compound C(C)C(CCC)(C)OCCO ZSUGETUFOUXQCL-UHFFFAOYSA-N 0.000 description 3
- XMJPURWAVZUBPM-UHFFFAOYSA-N 2-[2-(3-methylhexan-3-yloxy)propoxy]propan-1-ol Chemical compound C(C)C(CCC)(C)OC(C)COC(C)CO XMJPURWAVZUBPM-UHFFFAOYSA-N 0.000 description 3
- CIURCIMZEPBPPG-UHFFFAOYSA-N CC(CCC)OC(C)COC(C)CO Chemical compound CC(CCC)OC(C)COC(C)CO CIURCIMZEPBPPG-UHFFFAOYSA-N 0.000 description 3
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 3
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 238000007646 gravure printing Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- 239000001716 (4-methyl-1-propan-2-yl-1-cyclohex-2-enyl) acetate Substances 0.000 description 2
- PVMMVWNXKOSPRB-UHFFFAOYSA-N 1,2-dipropoxypropane Chemical compound CCCOCC(C)OCCC PVMMVWNXKOSPRB-UHFFFAOYSA-N 0.000 description 2
- GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 2
- QMGJMGFZLXYHCR-UHFFFAOYSA-N 1-(2-butoxypropoxy)butane Chemical compound CCCCOCC(C)OCCCC QMGJMGFZLXYHCR-UHFFFAOYSA-N 0.000 description 2
- VPYRPXKQBLKAPU-UHFFFAOYSA-N 1-(2-methylhexan-2-yloxy)propan-2-ol Chemical compound C(CC)CC(C)(C)OCC(C)O VPYRPXKQBLKAPU-UHFFFAOYSA-N 0.000 description 2
- HQSLKNLISLWZQH-UHFFFAOYSA-N 1-(2-propoxyethoxy)propane Chemical compound CCCOCCOCCC HQSLKNLISLWZQH-UHFFFAOYSA-N 0.000 description 2
- AMBINGYKZXBORB-UHFFFAOYSA-N 1-(3-methylhexan-3-yloxy)propan-2-ol Chemical compound C(C)C(CCC)(C)OCC(C)O AMBINGYKZXBORB-UHFFFAOYSA-N 0.000 description 2
- HMBWWRLRSBNRJS-UHFFFAOYSA-N 1-[1-(1-propoxypropan-2-yloxy)propan-2-yloxy]butane Chemical compound CCCCOC(C)COC(C)COCCC HMBWWRLRSBNRJS-UHFFFAOYSA-N 0.000 description 2
- UOWSVNMPHMJCBZ-UHFFFAOYSA-N 1-[2-(2-butoxypropoxy)propoxy]butane Chemical compound CCCCOCC(C)OCC(C)OCCCC UOWSVNMPHMJCBZ-UHFFFAOYSA-N 0.000 description 2
- BOGFHOWTVGAYFK-UHFFFAOYSA-N 1-[2-(2-propoxyethoxy)ethoxy]propane Chemical compound CCCOCCOCCOCCC BOGFHOWTVGAYFK-UHFFFAOYSA-N 0.000 description 2
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 2
- MCUPSZIPZGVKIB-UHFFFAOYSA-N 1-heptan-4-yloxypropan-2-ol Chemical compound C(CC)C(CCC)OCC(C)O MCUPSZIPZGVKIB-UHFFFAOYSA-N 0.000 description 2
- UVQCDDWFPNPHEQ-UHFFFAOYSA-N 1-hexan-3-yloxypropan-2-ol Chemical compound C(C)C(CCC)OCC(C)O UVQCDDWFPNPHEQ-UHFFFAOYSA-N 0.000 description 2
- JOERQAIRIDZWHX-UHFFFAOYSA-N 1-propoxy-2-(2-propoxypropoxy)propane Chemical compound CCCOCC(C)OCC(C)OCCC JOERQAIRIDZWHX-UHFFFAOYSA-N 0.000 description 2
- DBUMQODMPXCGAY-UHFFFAOYSA-N 2-(2-butan-2-yloxypropoxy)propan-1-ol Chemical compound CCC(C)OC(C)COC(C)CO DBUMQODMPXCGAY-UHFFFAOYSA-N 0.000 description 2
- SOHOWSNETCKHKH-UHFFFAOYSA-N 2-(2-heptan-4-yloxyethoxy)ethanol Chemical compound CCCC(CCC)OCCOCCO SOHOWSNETCKHKH-UHFFFAOYSA-N 0.000 description 2
- WDTSCGTYITZZEA-UHFFFAOYSA-N 2-(2-heptan-4-yloxypropoxy)propan-1-ol Chemical compound C(CC)C(CCC)OC(C)COC(C)CO WDTSCGTYITZZEA-UHFFFAOYSA-N 0.000 description 2
- XBIXRQVYHJWVOM-UHFFFAOYSA-N 2-(2-hexan-2-yloxypropoxy)propan-1-ol Chemical compound CC(CCCC)OC(C)COC(C)CO XBIXRQVYHJWVOM-UHFFFAOYSA-N 0.000 description 2
- WGYWCLNFFONDQZ-UHFFFAOYSA-N 2-(2-hexan-3-yloxyethoxy)ethanol Chemical compound CCCC(CC)OCCOCCO WGYWCLNFFONDQZ-UHFFFAOYSA-N 0.000 description 2
- CQGYCMPFUFLPQI-UHFFFAOYSA-N 2-(2-hexan-3-yloxypropoxy)propan-1-ol Chemical compound C(C)C(CCC)OC(C)COC(C)CO CQGYCMPFUFLPQI-UHFFFAOYSA-N 0.000 description 2
- KGRYJQHZLUAEES-UHFFFAOYSA-N 2-(2-methylbutan-2-yloxy)ethanol Chemical compound CCC(C)(C)OCCO KGRYJQHZLUAEES-UHFFFAOYSA-N 0.000 description 2
- PEBUZCNVNWGPAH-UHFFFAOYSA-N 2-(2-methylheptan-2-yloxy)ethanol Chemical compound CCCCCC(C)(C)OCCO PEBUZCNVNWGPAH-UHFFFAOYSA-N 0.000 description 2
- YUWVJKAIHWUMBS-UHFFFAOYSA-N 2-(2-methylhexan-2-yloxy)ethanol Chemical compound C(CC)CC(C)(C)OCCO YUWVJKAIHWUMBS-UHFFFAOYSA-N 0.000 description 2
- HBNHCGDYYBMKJN-UHFFFAOYSA-N 2-(4-methylcyclohexyl)propan-2-yl acetate Chemical compound CC1CCC(C(C)(C)OC(C)=O)CC1 HBNHCGDYYBMKJN-UHFFFAOYSA-N 0.000 description 2
- IBSOFCJIVZTVFX-UHFFFAOYSA-N 2-[2-(2,2-dimethylhexan-3-yloxy)ethoxy]ethanol Chemical compound CCCC(C(C)(C)C)OCCOCCO IBSOFCJIVZTVFX-UHFFFAOYSA-N 0.000 description 2
- IEJUWFNCWPVTEB-UHFFFAOYSA-N 2-[2-(2-methylheptan-2-yloxy)ethoxy]ethanol Chemical compound CCCCCC(C)(C)OCCOCCO IEJUWFNCWPVTEB-UHFFFAOYSA-N 0.000 description 2
- RQTLLMRLHWXVIU-UHFFFAOYSA-N 2-[2-(2-methylhexan-2-yloxy)ethoxy]ethanol Chemical compound C(CC)CC(C)(C)OCCOCCO RQTLLMRLHWXVIU-UHFFFAOYSA-N 0.000 description 2
- QSWXVRNYFLSGAA-UHFFFAOYSA-N 2-[2-(2-methylpentan-2-yloxy)ethoxy]ethanol Chemical compound CCCC(C)(C)OCCOCCO QSWXVRNYFLSGAA-UHFFFAOYSA-N 0.000 description 2
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- DSJBQZNFFIVOIS-UHFFFAOYSA-N CC(CC(C)OC(C)COC(C)CO)C Chemical compound CC(CC(C)OC(C)COC(C)CO)C DSJBQZNFFIVOIS-UHFFFAOYSA-N 0.000 description 1
- GJMVOGNRAITPJR-UHFFFAOYSA-N CC(CC(CCC)(C)OC(C)COC(C)CO)CC Chemical compound CC(CC(CCC)(C)OC(C)COC(C)CO)CC GJMVOGNRAITPJR-UHFFFAOYSA-N 0.000 description 1
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- MCHBCMILZSBXSH-UHFFFAOYSA-N CC(CCC(C(C)C)(C)OCCO)C Chemical compound CC(CCC(C(C)C)(C)OCCO)C MCHBCMILZSBXSH-UHFFFAOYSA-N 0.000 description 1
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- IVZDMJSOJSFEAK-UHFFFAOYSA-N CC(CCC(C(CC)C)OCC(C)O)C Chemical compound CC(CCC(C(CC)C)OCC(C)O)C IVZDMJSOJSFEAK-UHFFFAOYSA-N 0.000 description 1
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- JJESALXQUUNYRY-UHFFFAOYSA-N CC(CCC(CCC)(C)OCC(C)O)C Chemical compound CC(CCC(CCC)(C)OCC(C)O)C JJESALXQUUNYRY-UHFFFAOYSA-N 0.000 description 1
- VOAJHQWJCPHMLY-UHFFFAOYSA-N CC(CCC(CCC)(C)OCCO)C Chemical compound CC(CCC(CCC)(C)OCCO)C VOAJHQWJCPHMLY-UHFFFAOYSA-N 0.000 description 1
- ZWINCUUWXYTIIO-UHFFFAOYSA-N CC(CCC(CCC)(C)OCCOCCO)C Chemical compound CC(CCC(CCC)(C)OCCOCCO)C ZWINCUUWXYTIIO-UHFFFAOYSA-N 0.000 description 1
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- KZIUYMFPRUPMEI-UHFFFAOYSA-N CC(CCC)C(C(C)(C)C)OCC(C)O Chemical compound CC(CCC)C(C(C)(C)C)OCC(C)O KZIUYMFPRUPMEI-UHFFFAOYSA-N 0.000 description 1
- WXSKOZOILKSDGJ-UHFFFAOYSA-N CC(CCC)C(C(C)(C)C)OCCO Chemical compound CC(CCC)C(C(C)(C)C)OCCO WXSKOZOILKSDGJ-UHFFFAOYSA-N 0.000 description 1
- XNVYWCNMEXJSDN-UHFFFAOYSA-N CC(CCC)C(C(C)(C)C)OCCOCCO Chemical compound CC(CCC)C(C(C)(C)C)OCCOCCO XNVYWCNMEXJSDN-UHFFFAOYSA-N 0.000 description 1
- OVCJTIGMWBKGHD-UHFFFAOYSA-N CC(CCC)C(C(C)C)(C)OC(C)COC(C)CO Chemical compound CC(CCC)C(C(C)C)(C)OC(C)COC(C)CO OVCJTIGMWBKGHD-UHFFFAOYSA-N 0.000 description 1
- TWKZRWTVZGSQIL-UHFFFAOYSA-N CC(CCC)C(C(C)C)(C)OCC(C)O Chemical compound CC(CCC)C(C(C)C)(C)OCC(C)O TWKZRWTVZGSQIL-UHFFFAOYSA-N 0.000 description 1
- DSZZMHMRFLGNGL-UHFFFAOYSA-N CC(CCC)C(C(C)C)(C)OCCO Chemical compound CC(CCC)C(C(C)C)(C)OCCO DSZZMHMRFLGNGL-UHFFFAOYSA-N 0.000 description 1
- XWFPGMFXDZFBQE-UHFFFAOYSA-N CC(CCC)C(C(C)C)(C)OCCOCCO Chemical compound CC(CCC)C(C(C)C)(C)OCCOCCO XWFPGMFXDZFBQE-UHFFFAOYSA-N 0.000 description 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-UHFFFAOYSA-N 0.000 description 1
- NOTFZGFABLVTIG-UHFFFAOYSA-N Cyclohexylethyl acetate Chemical compound CC(=O)OCCC1CCCCC1 NOTFZGFABLVTIG-UHFFFAOYSA-N 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- FHADSMKORVFYOS-UHFFFAOYSA-N cyclooctanol Chemical compound OC1CCCCCCC1 FHADSMKORVFYOS-UHFFFAOYSA-N 0.000 description 1
- VBSHAXJPLHCYTH-UHFFFAOYSA-N cyclooctyl acetate Chemical compound CC(=O)OC1CCCCCCC1 VBSHAXJPLHCYTH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- YFPCLQKFNXUAAK-UHFFFAOYSA-N cyclopentyl acetate Chemical compound CC(=O)OC1CCCC1 YFPCLQKFNXUAAK-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 1
- 150000001983 dialkylethers Chemical class 0.000 description 1
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- UYAAVKFHBMJOJZ-UHFFFAOYSA-N diimidazo[1,3-b:1',3'-e]pyrazine-5,10-dione Chemical compound O=C1C2=CN=CN2C(=O)C2=CN=CN12 UYAAVKFHBMJOJZ-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- IMXBRVLCKXGWSS-UHFFFAOYSA-N methyl 2-cyclohexylacetate Chemical compound COC(=O)CC1CCCCC1 IMXBRVLCKXGWSS-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000006259 organic additive Substances 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- QZQLNUYDNNRPMA-UHFFFAOYSA-N propyl 2-cyclohexylacetate Chemical compound CCCOC(=O)CC1CCCCC1 QZQLNUYDNNRPMA-UHFFFAOYSA-N 0.000 description 1
- 229940116423 propylene glycol diacetate Drugs 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
- C04B41/81—Coating or impregnation
- C04B41/82—Coating or impregnation with organic materials
- C04B41/83—Macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/28—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/32—Polyethers, e.g. alkylphenol polyglycolether
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G4/00—Fixed capacitors; Processes of their manufacture
- H01G4/30—Stacked capacitors
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Power Engineering (AREA)
- Structural Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Ceramic Capacitors (AREA)
- Conductive Materials (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
- Paints Or Removers (AREA)
Description
1:セラミックスの粉末をポリビニルブチラール等のポリビニルアセタール樹脂又はアクリル樹脂等のバインダー樹脂と溶剤で分散させてスラリーとし、シート状に形成してグリーンシートを得る。
2:ニッケル、パラジウム等の導電性金属材料、エチルセルロース、及びターピネオール等の有機溶剤を主成分とする導体ペーストを、グリーンシート上に印刷法等により塗布し配線・塗膜を形成する。
3:上記導体ペースト中の有機溶剤を乾燥させる。
4:配線・塗膜が形成された積層シートを所定寸法に切断し、複数枚積み重ねて加熱圧着して積層体とする。
5:該積層体に電極等を取り付け、高温で焼成させると積層コンデンサが得られる。
で表される化合物を含有する積層セラミック部品製造用溶剤又は溶剤組成物を提供する。
本発明の積層セラミック部品製造用溶剤又は溶剤組成物は、上記式(1)で表される化合物を含有することを特徴とする。式(1)中、R1、R2は、同一又は異なって、直鎖状又は分岐鎖状アルキル基を示し、R1、R2のうち少なくとも一方は分岐鎖状アルキル基である。Aはアルキレン基を示す。nは1又は2である。
本発明の積層セラミック部品製造用溶剤又は溶剤組成物は、上記式(1)で表される化合物を含有することを特徴とする。
下記表1に記載の溶剤中に、ポリビニルブチラール樹脂として商品名「エスレックBL−S」(積水化学(株)製)、商品名「エスレックBL−1」(積水化学(株)製)、商品名「エスレックBH−3」(積水化学(株)製)及び、エチルセルロースとして商品名「エトセルSTD」(ダウ・ケミカル社製)をそれぞれ樹脂濃度が5重量%になるように添加し、液温65℃で3時間加熱溶解し、室温(25℃)で放冷した。
液温65℃で3時間加熱溶解操作を行った時点(下記表1で「65℃」と表記)と、その後、室温(25℃)で放冷した時点(下記表1で「室温」と表記)において、目視観察により各樹脂が各溶剤に対して溶解性を示すか否かを下記の基準で評価するとともに、各溶剤の溶剤性能を下記の基準で総合的に評価した。
<樹脂溶解性の評価基準>
◎:樹脂がすべて溶解した。
○:樹脂がほぼ溶解した。
△:樹脂が一部溶解した。
×:樹脂が不溶であった。
<溶剤性能の評価基準>
エチルセルロースに対して可溶解性を示し、ポリビニルブチラール樹脂に対して、室温(25℃)においても65℃においても不溶解性を示す溶剤:○
エチルセルロースに対して可溶解性を示し、ポリビニルブチラール樹脂に対して、室温(25℃)においては不溶解性を示すが、65℃においは可溶解性を示す溶剤:△
エチルセルロースに対して可溶解性を示すが、ポリビニルブチラール樹脂に対して、室温(25℃)においても65℃においても可溶解性を示す溶剤:×
DPMIPen:ジプロピレングリコールメチル−i−ペンチルエーテル(粘度:1.73mPa・s、ダイセル化学工業(株)製)
DPMIB:ジプロピレングリコールメチル−i−ブチルエーテル(粘度:1.48mPa・s、ダイセル化学工業(株)製)
DPMNP:ジプロピレングリコールメチル-n−プロピルエーテル(粘度:1.36mPa・s、ダイセル化学工業(株)製)
DHTA:ジヒドロターピニルアセテート(粘度:5.24mPa・s、商品名「メンタノールAC」、日本香料薬品(株)製)
Claims (2)
- ジプロピレングリコールメチルイソブチルエーテル、又はジプロピレングリコールメチルイソペンチルエーテルを少なくとも含有する積層セラミック部品製造用溶剤又は溶剤組成物。
- 積層セラミック部品が積層セラミックコンデンサである請求項1に記載の積層セラミック部品製造用溶剤又は溶剤組成物。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012018186A JP5973739B2 (ja) | 2011-04-13 | 2012-01-31 | 積層セラミック部品製造用溶剤又は溶剤組成物 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011088956 | 2011-04-13 | ||
JP2011088956 | 2011-04-13 | ||
JP2012018186A JP5973739B2 (ja) | 2011-04-13 | 2012-01-31 | 積層セラミック部品製造用溶剤又は溶剤組成物 |
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JP5886591B2 (ja) * | 2011-08-09 | 2016-03-16 | 株式会社ダイセル | 印刷用溶剤及びペースト組成物 |
WO2016117392A1 (ja) * | 2015-01-21 | 2016-07-28 | 株式会社ダイセル | 印刷法による電子部品製造用溶剤 |
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JP4965232B2 (ja) * | 2006-11-27 | 2012-07-04 | ナミックス株式会社 | 導電性ペースト |
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CN102731112A (zh) | 2012-10-17 |
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